| 1 | Fanconi anemia, Part 3. Cytogenetic monitoring in the bone marrow of patients with Fanconi anemia. | Coautor: Frias, S, Sánchez, S, Reyes, P, Barrera, MAM, et al. | 2024 | ACTA PEDIATRICA DE MEXICO | WoS-id: 001288658500010
Scopus-id: 2-s2.0-85201315562
| 1 | 1 |
| 2 | The Emerging Landscape of the Inherited Bone Marrow Failure Syndromes in Mexico | Coautor: Sosa, D, Gomez, ADR, Leal-Anaya, P, Juárez-Velázquez, R, et al. | 2024 | Blood | WoS-id: 001412489000006
| 0 | 0 |
| 3 | Estudio cromosómico de 303 pérdidas gestacionales en México | Coautor: Frías S., Garduño-Zarazúa L.M., Mayén D.G., Meléndez-Hernández R., et al. | 2024 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-85191736508
| 0 | 0 |
| 4 | Chromosome analysis of 303 pregnancy losses in Mexico; | Coautor: Frias S., Garduño-Zarazúa L.M., Mayén D.G., Meléndez-Hernández R., et al. | 2024 | GACETA MEDICA DE MEXICO | Scopus-id: 2-s2.0-85193542852
| 0 | 0 |
| 5 | Characterizing Chemotherapy/Radiotherapy-Induced Genome Chaos in Hodgkin's Lymphoma Patients Using M-FISH | 2ᵒ autor y autor de correspondencia: Frias S., Ramos S. | 2024 | Methods in Molecular Biology | Scopus-id: 2-s2.0-85196983804
| 0 | 0 |
| 6 | Profiling Chromosome Topological Features by Super-Resolution 3D Structured Illumination Microscopy | Coautor: Frias S., Fabian-Morales E., Rodríguez A., Gudiño A., et al. | 2024 | Methods in Molecular Biology | Scopus-id: 2-s2.0-85196997471
| 0 | 1 |
| 7 | Frequent copy number variants in a cohort of Mexican-Mestizo individuals | Coautor: Frias, Sara, Sanchez, Silvia, Juarez, Ulises, Dominguez, Julieta, et al. | 2023 | MOLECULAR CYTOGENETICS | WoS-id: 000912415900001
Scopus-id: 2-s2.0-85146115748
| 4 | 5 |
| 8 | Fanconi anemia, Part 2. Methodological strategy for molecular diagnosis in patients with Fanconi anemia | Coautor: Frias, Sara, Torres, Leda, Juarez, Ulises, Reyes, Pedro | 2023 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000951351000005
Scopus-id: 2-s2.0-85150722120
| 0 | 0 |
| 9 | A Boolean network model of the double-strand break repair pathway choice | Coautor: Frias, Sara, Ayala-Zambrano, Cecilia, Yuste, Mariana, Garcia-de-Teresa, Benilde, et al. | 2023 | JOURNAL OF THEORETICAL BIOLOGY | WoS-id: 001068786200001
Scopus-id: 2-s2.0-85169622136
| 4 | 4 |
| 10 | Inherited bone marrow failure syndromes: phenotype as a tool for early diagnostic suspicion at a major reference center in Mexico | Coautor: Frías S., Leal-Anaya P., Kimball T.N., Yanez-Felix A.L., et al. | 2023 | Frontiers in Genetics | WoS-id: 001158455000001
Scopus-id: 2-s2.0-85184465432
| 1 | 1 |
| 11 | Large-scale topological disruption of chromosome territories 9 and 22 is associated with nonresponse to treatment in CML | Coautor: Frias, Sara, Fabian-Morales, Eunice, Vallejo-Escamilla, David, Gudino, Adriana, et al. | 2022 | INTERNATIONAL JOURNAL OF CANCER | WoS-id: 000735749800001
Scopus-id: 2-s2.0-85122159292
| 4 | 6 |
| 12 | Fanconi anemia, Part 1. Cytogenetic diagnosis | Coautor y autor de correspondencia: FRIAS, SARA, MOLINA, BERTHA, Ramos, Sandra | 2022 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000791750600005
Scopus-id: 2-s2.0-85130907534
| 3 | 3 |
| 13 | Dysmorphology as a Clinical Tool for an Early Diagnosis of Fanconi Anemia | Coautor: FRIAS, SARA, Fiesco-Roa, Moises O., Gomez-Moreno, Paulina G., Espinosa-Curiel, Rubi M., et al. | 2022 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000791750600006
Scopus-id: 2-s2.0-85130915261
| 1 | 1 |
| 14 | The FA/BRCA Pathway; Cellular and Clinical Consequences of Its Failure | 1ᵉʳ autor y autor de correspondencia: Frias, Sara | 2022 | ENVIRONMENTAL AND MOLECULAR MUTAGENESIS | WoS-id: 000841940500057
| 0 | 0 |
| 15 | Fanconi anemia and dyskeratosis congenita/telomere biology disorders: Two inherited bone marrow failure syndromes with genomic instability | Coautor: Frías S., Fiesco-Roa M.Ó., García-de Teresa B., Leal-Anaya P., et al. | 2022 | Frontiers in Oncology | WoS-id: 000891738100001
Scopus-id: 2-s2.0-85137931063
| 18 | 21 |
| 16 | Fanconi Anemia Patients from an Indigenous Community in Mexico Carry a New Founder Pathogenic Variant in FANCG | Coautor: Frias S., Reyes P., García-De Teresa B., Juárez U., et al. | 2022 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | WoS-id: 000971202400001
Scopus-id: 2-s2.0-85124879348
| 9 | 9 |
| 17 | MYC Promotes Bone Marrow Stem Cell Dysfunction in Fanconi Anemia | Coautor: Frías S., Rodríguez A., Zhang K., Färkkilä A., et al. | 2021 | Cell Stem Cell | WoS-id: 000606536600009
Scopus-id: 2-s2.0-85092635441
| 40 | 43 |
| 18 | Inhibition of TGFß1 and TGFß3 promotes hematopoiesis in Fanconi anemia | Coautor: Frías S., Rodríguez A., Yang C., Furutani E., et al. | 2021 | EXPERIMENTAL HEMATOLOGY | WoS-id: 000615916900008
Scopus-id: 2-s2.0-85097098357
| 12 | 14 |
| 19 | Unravelling complex mosaicism of sex chromosomes in a patient with primary amenorrhea through cytogenetic analysis on urothelial cells | Coautor: FRIAS, SARA, Sevilla-Montoya, Rosalba, De Jesus Zavaleta-Abreu, Maria, Queipo, Gloria, et al. | 2021 | TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY | WoS-id: 000651121800025
Scopus-id: 2-s2.0-85103969317
| 1 | 2 |
| 20 | Heterogeneity and Clonal Evolution of Acquired PARP Inhibitor Resistance in TP53- and BRCA1-Deficient Cells | Coautor: FRIAS, SARA, Farkkila, Anniina, Rodriguez, Alfredo, Oikkonen, Jaana, et al. | 2021 | CANCER RESEARCH | WoS-id: 000651769000018
Scopus-id: 2-s2.0-85106190718
| 20 | 21 |
| 21 | Inherited Bone Marrow Failure Syndromes: etiology, pathophysiology, diagnosis, and management | Coautor: FRIAS, SARA, Fiesco-Roa, Moises, Monsivais-Orozco, Angelica, Rodriguez, Alfredo, et al. | 2021 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000681388700005
Scopus-id: 2-s2.0-85110277442
| 0 | 2 |
| 22 | Unclassified Chromosomal Abnormalities as an Indicator of Genomic Damage and Instability in Survivors of Hodgkin's Lymphoma. | Coautor y autor de correspondencia: Frias, S., Ramos, S., Molina, B. | 2021 | ENVIRONMENTAL AND MOLECULAR MUTAGENESIS | WoS-id: 000687648100130
| 0 | 0 |
| 23 | Non-classical 1p36 deletion in a patient with Duane retraction syndrome: case report and literature review | Coautor: FRIAS, SARA, Yokoyama, Emiy, Villarroel, Camilo E., Diaz, Sinhue, et al. | 2020 | MOLECULAR CYTOGENETICS | WoS-id: 000571115500001
Scopus-id: 2-s2.0-85091273525
| 3 | 3 |
| 24 | Microcephaly: diagnostic considerations | Coautor: FRIAS, SARA, Garza-Mayen, Gilda, Fiesco-Roa, Moises, Garcia-de Teresa, Benilde | 2020 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000574286600005
Scopus-id: 2-s2.0-85092281719
| 2 | 1 |
| 25 | Chromosome instability in fanconi anemia: From breaks to phenotypic consequences | Coautor y autor de correspondencia: Frias S., García-De-teresa B., Rodríguez A. | 2020 | GENES | WoS-id: 000602152400001
Scopus-id: 2-s2.0-85098764297
| 51 | 53 |
| 26 | Meiotic susceptibility for induction of sperm with chromosomal aberrations in patients receiving combination chemotherapy for Hodgkin lymphoma | 1ᵉʳ autor: Frias, Sara, Van Hummelen, Paul, Meistrich, Marvin L., Wyrobek, Andrew J. | 2020 | PLOS ONE | WoS-id: 000603611900007
Scopus-id: 2-s2.0-85099114693
| 2 | 3 |
| 27 | Nonclonal Chromosome Aberrations and Genome Chaos in Somatic and Germ Cells from Patients and Survivors of Hodgkin Lymphoma | 1ᵉʳ autor: Frias, Sara, Ramos, Sandra, Salas, Consuelo, Molina, Bertha, et al. | 2019 | GENES | WoS-id: 000459743800037
Scopus-id: 2-s2.0-85060618157
| 16 | 23 |
| 28 | Low bone mineral density and renal malformation in Mexican patients with Turner syndrome are associated with single nucleotide variants in vitamin D-metabolism genes | 2ᵒ autor: Frias, Sara, Barrientos-Rios, Rehotbevely, Velazquez-Aragon, Jose A., Villaroel, Camilo E., et al. | 2019 | GYNECOLOGICAL ENDOCRINOLOGY | WoS-id: 000461972100001
Scopus-id: 2-s2.0-85063099458
| 4 | 5 |
| 29 | Genomic chaos in peripheral blood lymphocytes of hodgkins lymphoma patients 1 year after ABVD chemotherapy/radiotherapy | 1ᵉʳ autor y autor de correspondencia: Frias S. | 2019 | ENVIRONMENTAL AND MOLECULAR MUTAGENESIS | WoS-id: 000462888300008
Scopus-id: 2-s2.0-85063678092
| 2 | 0 |
| 30 | WIP1 Contributes to the Adaptation of Fanconi Anemia Cells to DNA Damage as Determined by the Regulatory Network of the Fanconi Anemia and Checkpoint Recovery Pathways | Coautor: Frías S., Rodríguez A., Jesús Naveja J., Torres L., et al. | 2019 | Frontiers in Genetics | WoS-id: 000467461500003
Scopus-id: 2-s2.0-85067855840
| 5 | 5 |
| 31 | Atorvastatin and Fenofibrate Increase the Content of Unsaturated Acyl Chains in HDL and Modify In Vivo Kinetics of HDL-Cholesteryl Esters in New Zealand White Rabbits | Coautor: Frías S., Flores-Castillo C., Luna-Luna M., Carreón-Torres E., et al. | 2019 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | WoS-id: 000471001400152
Scopus-id: 2-s2.0-85066818433
| 8 | 8 |
| 32 | FANCC Dutch founder mutation in a Mennonite family from Tamaulipas, México | 2ᵒ autor: Frias S., García-de Teresa B., Molina B., Villarreal M.T., et al. | 2019 | Molecular Genetics & Genomic Medicine | WoS-id: 000476745400049
Scopus-id: 2-s2.0-85067281483
| 8 | 8 |
| 33 | Presence of 15p Marker D15Z1 on the Short Arm of Acrocentric Chromosomes is Associated with Aneuploid Offspring in Mexican Couples | Coautor: Frias, Sara, Ramos, Sandra, Rodriguez, Rebeca, Castro, Oscar, et al. | 2019 | INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES | WoS-id: 000498946100009
Scopus-id: 2-s2.0-85074168947
| 3 | 2 |
| 34 | Derivative chromosomes involving 5p large rearranged segments went unnoticed with the use of conventional cytogenetics | Coautor: Frías S., Yokoyama E., Del Castillo V., Sánchez S., et al. | 2018 | MOLECULAR CYTOGENETICS | WoS-id: 000431897500002
Scopus-id: 2-s2.0-85046671603
| 5 | 6 |
| 35 | Fanconi Anemia and Laron Syndrome | 2ᵒ autor y autor de correspondencia: Frias, Sara, Garcia-de Teresa, Benilde | 2018 | AMERICAN JOURNAL OF THE MEDICAL SCIENCES | WoS-id: 000434946600019
Scopus-id: 2-s2.0-85048591384
| 0 | 0 |
| 36 | ROLE OF KLOTHO RS9536282 GENE POLYMORPHISM ON BMD IN MEXICAN CHILDREN AND ADOLESCENT WITH TURNER SYNDROME | Coautor: Frias, F. S., Altamirano-Bustamante, N. A. B., Torres-Maldonado, L. T. M., Banrrientos-Rios, R. B. R., et al. | 2018 | OSTEOPOROSIS INTERNATIONAL | WoS-id: 000440102404174
| 0 | 0 |
| 37 | Genomic chaos in peripheral blood lymphocytes of Hodgkin's lymphoma patients one year after ABVD chemotherapy/radiotherapy | Coautor: Frias, Sara, Ramos, Sandra, Navarrete-Meneses, Pilar, Molina, Bertha, et al. | 2018 | ENVIRONMENTAL AND MOLECULAR MUTAGENESIS | WoS-id: 000447275100008
Scopus-id: 2-s2.0-85052954475
| 12 | 15 |
| 38 | Heterogeneous Diagnoses Underlying Radial Ray Anomalies | Coautor: Frías, S., Sevilla-Montoya, R., Aguinaga, M., Martínez, A., et al. | 2017 | INDIAN JOURNAL OF PEDIATRICS | WoS-id: 000398000300005
Scopus-id: 2-s2.0-85006427909
| 2 | 4 |
| 39 | DNA Damage as a Driver for Growth Delay: Chromosome Instability Syndromes with Intrauterine Growth Retardation | Coautor y autor de correspondencia: Frias, Sara, Garcia-de Teresa, Benilde, Hernandez-Gomez, Mariana | 2017 | BIOMED RESEARCH INTERNATIONAL | WoS-id: 000414993300001
Scopus-id: 2-s2.0-85042095636
| 12 | 15 |
| 40 | 7p15 deletion as the cause of hand-foot-genital syndrome: A case report, literature review and proposal of a minimum region for this phenotype | Coautor: Frias, Sara, Yokoyama, Emiy, Lesley Smith-Pellegrin, Dennise, Sanchez, Silvia, et al. | 2017 | MOLECULAR CYTOGENETICS | WoS-id: 000415335600001
Scopus-id: 2-s2.0-85034453724
| 3 | 5 |
| 41 | Cytogenetic and Cytogenomic Approach of patients with Intellectual Disability and Congenital Malformations | 2ᵒ autor: Frias, S., Yokoyama-Rebollar, E., Del Castillo-Ruiz, V | 2017 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000416317300010
| 1 | 0 |
| 42 | Abordaje citogenético y citogenómico de pacientes con discapacidad intelectual y malformaciones congénitas | 2ᵒ autor: FrÃas S., Yokoyama-Rebollar E., Del Castllo-Ruiz V. | 2017 | ACTA PEDIATRICA DE MEXICO | Scopus-id: 2-s2.0-85040685878
| 0 | 1 |
| 43 | Multidisciplinary approach of the Fanconi anemia patient | Coautor y autor de correspondencia: Frias, Sara, Garcia de Teresa, Benilde, Rodriguez, Alfredo | 2016 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000370327500008
Scopus-id: 2-s2.0-84989948157
| 0 | 0 |
| 44 | 5q34q35.3 duplication involving the NSD1 gene: region defined by microarray CGH. A case report. | Coautor: Frias-Vazquez, S., Vazquez-del Campo, A. R., Torres-Maldonado, L., Sanchez-Sandoval, S., et al. | 2016 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000388796700004
Scopus-id: 2-s2.0-84989934788
| 1 | 2 |
| 45 | Microarray analysis of microRNA expression in mouse fetus at 13.5 and 14.5 days post-coitum in ear and back skin tissues | Coautor: Frias, Sara, Torres, Leda, Juarez, Ulises, Garcia, Laura, et al. | 2016 | Genomics Data | WoS-id: 000395318100035
Scopus-id: 2-s2.0-84976339905
| 1 | 1 |
| 46 | Persistence of chromosomal aberrations in peripheral blood lymphocytes of Hodgkin's lymphoma patients after ABVD chemotherapy | Coautor: Frias, S., Ramos, S., Navarrete, P., Molina, B., et al. | 2016 | TOXICOLOGY LETTERS | WoS-id: 000396848100449
| 0 | 0 |
| 47 | NFE2L2 Gene Variants and Arsenic Susceptibility: A Lymphoblastoid Model | Coautor: Frías S., Morales-Marin M.E., Cordova E.J., Centeno F., et al. | 2015 | JOURNAL OF TOXICOLOGY AND ENVIRONMENTAL HEALTH-PART A-CURRENT ISSUES | WoS-id: 000355600400002
Scopus-id: 2-s2.0-84930591461
| 4 | 3 |
| 48 | Hydroxyurea induces chromosomal damage in G2 and enhances the clastogenic effect of mitomycin C in Fanconi anemia cells | Coautor: Frias S., Molina B., Marchetti F., Gómez L., et al. | 2015 | ENVIRONMENTAL AND MOLECULAR MUTAGENESIS | WoS-id: 000356426200004
Scopus-id: 2-s2.0-84931043203
| 6 | 6 |
| 49 | Fanconi anemia cells with unrepaired DNA damage activate components of the checkpoint recovery process | Coautor: Frías S., Rodríguez A., Torres L., Juárez U., et al. | 2015 | THEORETICAL BIOLOGY AND MEDICAL MODELLING | WoS-id: 000361668200001
Scopus-id: 2-s2.0-84941771494
| 13 | 14 |
| 50 | A Boolean network model of human gonadal sex determination | 2ᵒ autor: Frias S., Ríos O., Rodríguez A., Kofman S., et al. | 2015 | THEORETICAL BIOLOGY AND MEDICAL MODELLING | WoS-id: 000364754700001
Scopus-id: 2-s2.0-84960333621
| 37 | 38 |
| 51 | Identification of cryptic translocations in acrocentric chromosomes from aneuploid miscarriages | Coautor: Frias, Sara, Ramos, Sandra, Molina, Bertha, Grether, Patricia, et al. | 2015 | ACTA PEDIATRICA DE MEXICO | WoS-id: 000370325300002
Scopus-id: 2-s2.0-84994056280
| 1 | 1 |
| 52 | External ear microRNA expression profiles during mouse development | Coautor: Frias S., Torres L., Juárez U., García L., et al. | 2015 | INTERNATIONAL JOURNAL OF DEVELOPMENTAL BIOLOGY | WoS-id: 000372858700011
Scopus-id: 2-s2.0-84961298567
| 12 | 12 |
| 53 | Interstitial Deletion of 2q24.2: Further Delineation of an Emerging Syndrome Associated With Intellectual Disability, Severe Hypotonia and Moderate Intrauterine Growth Restriction | Coautor: Frías S., Yokoyama E., Villarroel C.E., Del Castillo V., et al. | 2014 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000331978700038
Scopus-id: 2-s2.0-84894226111
| 1 | 1 |
| 54 | RAD50 targeting impairs DNA damage response and sensitizes human breast cancer cells to cisplatin therapy | Coautor: Frías S., Flores-Pérez A., Rafaelli L.E., Ramírez-Torres N., et al. | 2014 | CANCER BIOLOGY & THERAPY | WoS-id: 000337169500015
Scopus-id: 2-s2.0-84901719361
| 18 | 21 |
| 55 | La mitosis y su regulación | 2ᵒ autor y autor de correspondencia: Frias-Vázquez S., De Jesús Rodríguez-Gómez A. | 2014 | ACTA PEDIATRICA DE MEXICO | Scopus-id: 2-s2.0-84930800411
| 0 | 0 |
| 56 | Microtia-atresia: Aspectos clínicos, genéticos y genómicos | 2ᵒ autor: Frías S., Aguinaga-Ríos M., Arenas-Aranda D.J., Morán-Barroso V.F. | 2014 | BOLETIN MEDICO DEL HOSPITAL INFANTIL DE MEXICO | Scopus-id: 2-s2.0-84938081632
| 0 | 5 |
| 57 | Detection of Cryptic Translocations of Acrocentric Chromosomes in Couples with Normal Descendants or Aneuploid Miscarriages. | 1ᵉʳ autor: Frias, S, Ramos, S, Castro, O, Molina, B, et al. | 2013 | ENVIRONMENTAL AND MOLECULAR MUTAGENESIS | WoS-id: 000323429400093
| 0 | 0 |
| 58 | A Boolean network model of the FA/BRCA pathway | Coautor: Frias, S, Rodriguez, A, Sosa, D, Torres, L, et al. | 2012 | Bioinformatics | WoS-id: 000301972900015
Scopus-id: 2-s2.0-84859054645
| 34 | 37 |
| 59 | Persistent genomic instability in peripheral blood lymphocytes from hodgkin lymphoma survivors | Coautor: Frias S., Salas C., Niembro A., Lozano V., et al. | 2012 | ENVIRONMENTAL AND MOLECULAR MUTAGENESIS | WoS-id: 000302612800003
Scopus-id: 2-s2.0-84859614012
| 16 | 17 |
| 60 | Genetic abnormalities in leukemia secondary to treatment in patients with Hodgkin's disease | Coautor y autor de correspondencia: Frías S., Salas C., Pérez-Vera P. | 2011 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000290049900009
Scopus-id: 2-s2.0-79955844782
| 10 | 12 |
| 61 | An assessment of immediate DNA damage to occupationally exposed workers to low dose ionizing radiation by using the comet assay | Coautor: Frías S., Martínez A., Coleman M., Romero-Talamás C.A. | 2010 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: 000276827400004
Scopus-id: 2-s2.0-77952154323
| 12 | 14 |
| 62 | Differential-associative processing: A new strategy for learning highly-similar concepts | Coautor: Frias S., Hannon B., Lozano G., Picallo-Hernandez S., et al. | 2010 | APPL COGNITIVE PSYCH | WoS-id: 000284713600003
Scopus-id: 2-s2.0-78649603901
| 2 | 2 |
| 63 | Acrocentric cryptic translocation associated with nondisjunction of chromosome 21 | Coautor: Frias S., Ramos S., Alcántara M.A., Molina B., et al. | 2008 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000252126300015
Scopus-id: 2-s2.0-37549028330
| 5 | 7 |
| 64 | Multiple copies of RUNX1: description of 14 new patients, follow-up, and a review of the literature | Coautor: Frías S., Pérez-Vera P., Montero-Ruíz O., Rivera-Luna R., et al. | 2008 | CANCER GENET CYTOGEN | WoS-id: 000252841800006
Scopus-id: 2-s2.0-38349060647
| 11 | 12 |
| 65 | Analysis of gene rearrangements using a fluorescence in situ hybridization method in Mexican patients with acute lymphoblastic leukemia: experience at a single institution | Coautor: Frías S., Pérez-Vera P., Salas C., Montero-Ruiz O., et al. | 2008 | CANCER GENET CYTOGEN | WoS-id: 000257976300003
Scopus-id: 2-s2.0-46449098873
| 10 | 11 |
| 66 | Local and circulating microchimerism is associated with hypersensitivity pneumonitis | 2ᵒ autor: Frías S., Bustos M.L., Ramos S., Estrada A., et al. | 2007 | AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE | WoS-id: 000247549800014
Scopus-id: 2-s2.0-34447279648
| 21 | 29 |
| 67 | Unusual mixed gonadal dysgenesis associated with Müllerian duct persistence, polygonadia, and a 45,X/46,X,idic(Y)(p) karyotype | Coautor: Frías S., Queipo G., Nieto K., Grether P., et al. | 2005 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000230949400018
Scopus-id: 2-s2.0-23044484449
| 9 | 9 |
| 68 | Detection of ETV6 and RUNX1 gene rearrangements using fluorescence in situ hybridization in Mexican patients with acute lymphoblastic leukemia: Experience at a single institution | Coautor: Frías S., Pérez-Vera P., Montero-Ruiz O., Ulloa-Avilés V., et al. | 2005 | CANCER GENET CYTOGEN | WoS-id: 000233292800008
Scopus-id: 2-s2.0-26444585899
| 11 | 11 |
| 69 | DEB Test for Fanconi Anemia Detection in Patients with Atypical Phenotypes | Coautor: Frias S., Esmer C., Sánchez S., Ramos S., et al. | 2004 | AMERICAN JOURNAL OF MEDICAL GENETICS PART A | WoS-id: 000187282500005
Scopus-id: 2-s2.0-0942276983
| 41 | 44 |
| 70 | A Strategy to Detect Chromosomal Abnormalities in Children with Acute Lymphoblastic Leukemia | 2ᵒ autor: Frías S., Pérez-Vera P., Carnevale A., Betancourt M., et al. | 2004 | JOURNAL OF PEDIATRIC HEMATOLOGY ONCOLOGY | Scopus-id: 2-s2.0-17744407920
| 0 | 10 |
| 71 | NOVP chemotherapy for Hodgkin's disease transiently induces sperm aneuploidies associated with the major clinical aneuploidy syndromes involving chromosomes X, Y, 18, and 21 | 1ᵉʳ autor: Frias S., Van Hummelen P., Meistrich M.L., Lowe X.R., et al. | 2003 | CANCER RESEARCH | WoS-id: 000180290500010
Scopus-id: 2-s2.0-0037226446
| 55 | 66 |
| 72 | Regional consideration in patient access to emergency contraception | 1ᵉʳ autor: Frias S., Sommers D.K., Augereau L. | 2003 | Drugs and Therapy Perspectives | Scopus-id: 2-s2.0-0042880998
| 0 | 0 |
| 73 | The clastogenic response of the 1q12 heterochromatic region to DNA cross-linking agents is independent of the Fanconi anaemia pathway | Coautor: Frias S., Callén E., Ramírez M.J., Creus A., et al. | 2002 | Carcinogenesis | WoS-id: 000177231000002
Scopus-id: 2-s2.0-0036045399
| 5 | 5 |
| 74 | Detection of mosaicism in lymphocytes of parents of free trisomy 21 offspring | 1ᵉʳ autor: Frias S., Ramos S., Molina B., Del Castillo V., et al. | 2002 | MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS | WoS-id: 000178627800003
Scopus-id: 2-s2.0-0037179494
| 14 | 13 |
| 75 | Cytogenetics in acute lymphoblastic leukemia in Mexican children: An institutional experience | Coautor: Frías S., Pérez-Vera P., Mújica-Sánchez M., Carnevale A., et al. | 2001 | Archives Of Medical Research | WoS-id: 000169230700005
Scopus-id: 2-s2.0-0034986629
| 14 | 16 |
| 76 | Clinical and cytogenetic variability on twelve Fanconi anemia families and its relationship with complementation group assignment [Variabilidad clínica y citogenética en doce familias mexicanas con anemia de Fanconi y su relación con el g | Coautor: Frías Vázquez S., Esmer Sánchez M.D.C., Carnevale Cantoni A., Molina Álvarez B., et al. | 1999 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | Scopus-id: 2-s2.0-0012832388
| 0 | 2 |
| 77 | Chromosome instability with bleomycin and x-ray hypersensitivity in a boy with Nijmegen breakage syndrome | Coautor: Frías S., Pérez-Vera P., Angel A.G.-D., Molina B., et al. | 1997 | AM J MED GENET | WoS-id: A1997WV78400005
Scopus-id: 2-s2.0-0030997558
| 10 | 11 |
| 78 | Delayed repair of DNA damage by ionizing radiation in cells from patients with juvenile systemic lupus erythematosus and rheumatoid arthritis | Coautor: Frias S., McCurdy D., Tai L.-Q., Wang Z. | 1997 | RADIATION RESEARCH | WoS-id: A1997WA76700007
Scopus-id: 2-s2.0-0031021258
| 72 | 79 |
| 79 | Fluorescence in situ hibridization in six patients with chromosome 18 structural aberrations and in seven patients with marker chromosomes [Hibridación in situ con fluorescencia en seis pacientes con alteraciones del cromosoma 18 y en siete | Coautor: Frías S., Esmer M.D.C., Carnevale A., Gómez L., et al. | 1996 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1996UD85200004
Scopus-id: 2-s2.0-0029690630
| 1 | 1 |
| 80 | Effect of hydroxyurea and normal plasma on DNA synthesis in lymhocytes from Fanconi anemia patient | 1ᵉʳ autor: Frias S., Gómez L., Molina B., Rojas E., et al. | 1996 | MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS | WoS-id: A1996VM36400014
Scopus-id: 2-s2.0-0030601664
| 9 | 9 |
| 81 | Detection of aneuploidies in buccal mucosa by in situ hybridization [Detección de aneuploidías por hibridación in situ en células de mucosa oral] | 1ᵉʳ autor: Frías S., Ordaz G., Blanco B., Molina B., et al. | 1996 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | Scopus-id: 2-s2.0-3242850940
| 0 | 1 |
| 82 | Tetrasomy 18p in two cases confirmation by in situ hybridization | 2ᵒ autor: Frias S., Del Carmen Esmer M., Gomez L., Carnevale A. | 1994 | ANN GENET-PARIS | WoS-id: A1994PZ40500010
Scopus-id: 2-s2.0-0028588455
| 5 | 5 |
| 83 | Effects of the addition of conditioned media on the response of Fanconi anemia lymphocytes to mitomycin C [EFECTO DE LA ADICION DE MEDIOS CONDICIONADOS SOBRE LA RESPUESTA DE LOS LINFOCITOS DE ANEMIA DE FANCONI A LA MITOMICINA-C] | 1ᵉʳ autor: Frias S., Molina B., Gomez L., Carnevale A. | 1992 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1992KF59600006
Scopus-id: 2-s2.0-0027008384
| 2 | 2 |
| 84 | Effect of mitomycin C and bromodeoxyuridine on Fanconi anemia lymphocytes | 1ᵉʳ autor: Frias S., Mendoza S., Molina B., Carnevale A. | 1991 | ANN GENET-PARIS | WoS-id: A1991GL04100011
Scopus-id: 2-s2.0-0026001403
| 2 | 3 |
| 85 | Effect of gamma radiations on robertsonian translocations [Acción de las radiaciones gama sobre las traslocaciones robertsonianas.] | Coautor: Frías S., Ortiz de Zárate G., Carnevale A., Molina B., et al. | 1991 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | Scopus-id: 2-s2.0-0026146637
| 0 | 2 |
| 86 | Mitomycin C action on the fusion points of reciprocal translocations [ACCION DE LA MITOMICINA C (MMC) SOBRE LOS PUNTOS DE FUSION DE TRANSLOCACIONES RECIPROCAS] | 2ᵒ autor: Frias S., Molina B., Carnevale A. | 1990 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1990DT25700006
Scopus-id: 2-s2.0-0025145995
| 0 | 0 |
| 87 | Synergism of BrdU and mitomycin C on the production of chromosome aberrations in Fanconi's anemia | 1ᵉʳ autor: Frias S., Molina B., Carnevale A. | 1989 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1989U314000005
Scopus-id: 2-s2.0-0024400730
| 3 | 1 |
| 88 | Mitomycin C effect on Robertsonian translocations | 1ᵉʳ autor: Frias S., Carnevale A., De Jesus Zavaleta M., Molina B. | 1988 | ANN GENET-PARIS | WoS-id: A1988P982900005
Scopus-id: 2-s2.0-0023748425
| 2 | 3 |
| 89 | Genetic heterogenicity study in Fanconi's anemia by the addition of plasma [Estudio de heterogeneidad genética en anemia de Fanconi por medio de la adición de plasma.] | 1ᵉʳ autor: Frías S., Carnevale A., Molina B., del Castillo V. | 1986 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1986E530800005
Scopus-id: 2-s2.0-0011878429
| 2 | 1 |
| 90 | Effect of cocultivation and addition of normal plasma on the response to mitomycin C in Fanconi's anemia lymphocytes [Efecto de la cocultivación y la adición de plasma normal sobre la respuesta a la mitomicina C de los linfocitos de anemia | 2ᵒ autor y autor de correspondencia: Frías S., Carnevale A. | 1985 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1985AGR8100007
Scopus-id: 2-s2.0-0011875820
| 2 | 2 |
| 91 | Partial trisomy 16q resulting from maternal translocation 11p/16q | 2ᵒ autor: Frias S., Calva P., Carnevale A., Reyes P. | 1984 | ANN GENET-PARIS | WoS-id: A1984SY44600014
Scopus-id: 2-s2.0-0021245493
| 20 | 20 |
| 92 | Interstitial deletion of the long arm of chromosome 13 | 2ᵒ autor: Frias S., Carnevale A., Alcantar R. | 1984 | ANN GENET-PARIS | WoS-id: A1984SM17200009
Scopus-id: 2-s2.0-0021348864
| 14 | 14 |
| 93 | Use of a test exposing lymphocytes to mitomycin C in the diagnosis of Fanconi's anemia [Utilidad de la prueba de exposición de linfocitos a mitomicina C en el diagnóstico de anemia de Fanconi.] | 1ᵉʳ autor: Frías S., Carnevale A., del Castillo V. | 1984 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1984TT13200002
Scopus-id: 2-s2.0-0347412094
| 4 | 3 |
| 94 | Cell cycle in normal individuals and in patients with Down, cri-du-chat and Turner syndromes | 1ᵉʳ autor: Frias S., Carnevale A. | 1983 | ANN GENET-PARIS | Scopus-id: 2-s2.0-0020640071
| 0 | 9 |
| 95 | C band polymorphisms of chromosomes 1, 9 and 16 in families with children with Down's syndrome (author's transl) [Polimorfísmos de bandas C en los cromosomas 1, 9 y 16 en familias con hijos con trisomía 21 por no disyunción.] | Coautor: Frías S., Blanco B., Castillo J., Carnevale A. | 1982 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1982NJ39200010
Scopus-id: 2-s2.0-0020008722
| 1 | 0 |
| 96 | A clinical syndrome associated with Dup(5p) | Coautor: Frías S., Carnevale A., Hernandez M., Limon-Toledo I., et al. | 1982 | AM J MED GENET | WoS-id: A1982PQ77600007
Scopus-id: 2-s2.0-0020378360
| 26 | 27 |
| 97 | Cytogenetics in pediatric practice. Experience of 10 years (author's transl) [La citogenética en pediatría. Experiencia de 10 años.] | Coautor: Frías S., Carnevale A., Blanco B., Castillo J., et al. | 1981 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1981LW67300007
Scopus-id: 2-s2.0-0019551727
| 0 | 0 |
| 98 | Identification of chromosome anomalies by G banding in patients with apparently normal karyotype (author's transl) [Identificación de anormalidades cromosómicas por la técnica de bandas G en pacientes con cariotipo aparentemente normal co | 2ᵒ autor: Frías S., Carnevale A., del Castillo V. | 1978 | REVISTA DE INVESTIGACION CLINICA-CLINICAL AND TRANSLATIONAL INVESTIGATION | WoS-id: A1978FF08700002
Scopus-id: 2-s2.0-0017954407
| 0 | 0 |
| 99 | Partial trisomy of the short arm of chromosome 7 due to a familial translocation rcp(7;14) (p11;p11) | 2ᵒ autor: Frías S., Carnevale A., Del Castillo V. | 1978 | CLINICAL GENETICS | WoS-id: A1978FW99000002
Scopus-id: 2-s2.0-0018169776
| 34 | 27 |
| 100 | Identification of chromosomal abnormalities by trypsin C banding in 100 patients with normal karyotype by conventional techniques [FIFTH INTERNATIONAL CONGRESS OF HUMAN GENETICS] | 1ᵉʳ autor: Frias S., Carnevale A., Monroy E., Del Castillo V. | 1976 | Excerpta Med., Amsterdam, I.C.S. | Scopus-id: 2-s2.0-0017041640
| 0 | 0 |
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